Isobornyl Acetate
  • Isobornyl AcetateIsobornyl Acetate

Isobornyl Acetate

Isobornyl acetate;IBA's cas code is 125-12-2

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Isobornylacetat Grunnleggende informasjon


Description References


Product Name:

Isobornylacetat

Synonymer:

ISOBORNYLACETAT; BORNYLACETATE (ISO); 2-CAMPHANYL ACETATE; 2-BORNANOL: ACETATE, EXO; 1,7,7-trimetyl-, acetat, exo-bicyklo (2.2.1) heptan-2-o; 1,7, 7-trimetyl-, acetat, exo-bicyklo [2.2.1] heptan-2-o; Pichtosin; 1,7,7-trimetyl-, acetat, exo-Bicyclo [2.2.1] heptan-2-ol

CAS:

125-12-2

MF:

C12H20O2

MW:

196.29

EINECS:

204-727-6

Produkt kategorier:

FINE Chemical & INTERMEDIATES;Aroma Chemicals;Bicyclic Monoterpenes;Biochemistry;Terpenes;Alphabetical Listings;Flavors and Fragrances;I-L

Mol-fil:

125-12-2.mol



Isobornyl acetate Chemical Properties


Melting point 

29 ° C

Boiling point 

229-233 ° C (lys)

density 

0.983 g/mL at 25 °C(lit.)

damptrykk

0,13 hPa (20 ° C)

brytningsindeks

n20 / D 1.4635 (lys.)

FEMA 

2160 | ISOBORNYL ACETATE

Fp 

190 °F

storage temp. 

Store below +30°C.

løselighet

0.16g/l

Spesifikk tyngdekraft

0.98

Vannløselighet

Not miscible or difficult to mix with water.

JECFA Number

1388

BRN 

3197572

Stability:

Stable. Flammable. Incompatible with strong oxidizing agents.

InChIKey

XWIGWPJZNFZLBG-UHFFFAOYSA-N

CAS DataBase Reference

125-12-2 (CAS DataBase Reference)

NIST Chemistry Reference

Isobornylacetat (125-12-2)

EPA Substance Registry System

Isobornyl acetate (125-12-2)


Isobornyl acetate Safety Information


Hazard Codes 

Xi

Risk Statements 

36/37 / 38-38

Sikkerhetserklæringer

26-36/37/39-24/25

WGK Tyskland

1

RTECS 

NP7350000

Selvantennelsestemperatur

440 ° C DIN 51794

TSCA

Yes

HS Code 

29153900

Toxicity

LD50 orally in Rabbit: > 10000 mg/kg LD50 dermal Rabbit > 20000 mg/kg


Isobornyl acetate Usage And Synthesis


Description

Isobornylacetat er en slags acetatester. Den kan produseres gjennom forestringen mellom acetat og kamfen. Det er et slags smaksstoff med duft, og kan brukes som mellomprodukt som trengs for å produsere medisinsk syntetisk kamfer.

Referanser

Ning, Chunli, et al. "Study on the catalyst for the synthesis of isobornyl acetate." Industrial Catalysis (2012). Opdyke, D. L. J. "Monographs on fragrance raw materials: Isobornyl acetate." Food & Cosmetics Toxicology 13.5(1975): 552-552. Chimal-Valencia, O, et al. "Ion exchange resins as catalyst for the isomerization of alpha-pinene to camphene. " Bioresource Technology 93.2(2004): 119-123.

Description

Isobornyl acetate has a pleasant, camphor-like odor reminiscent of some varieties of pine needles and hemlock, and a fresh, burning taste. May be prepared by treatment of camphene with acetic acid, usually in the presence of a catalyst; also by acetylation of isobomeol; depending on the starting material (d-camphene or ι-camphene), the resulting acetate may exhibit a slight optical activity; the commercial product is considered to be optically inactive.

Kjemiske egenskaper

Isobornylacetat har en behagelig, kamferaktig lukt som minner om noen varianter av pinjenåler og hemlock og en frisk, brennende smak

Kjemiske egenskaper

Fargeløs væske; lukt av furunål. Løselig i de fleste faste oljer og mineraloljer; uoppløselig inglyserol og vann. Brennbar.

Kjemiske egenskaper

Isobornyl Acetate has been identified in a number of essential oils. It is a colorless liquid with a pleasant, pine-needle odor. Isobornyl acetate is prepared from camphene and acetic acid in the presence of acidic catalysts (e.g., sulfuric acid) or on a styrene–divinylbenzene acid ion-exchanger.
Isobornylacetat brukes i store mengder for parfymering av såper, badeprodukter og luftfriskere. Imidlertid er den viktigste bruken av isobornylacetat som et mellomprodukt i produksjonen av kamfer.

Uses

Sammensatt lukt av furu-nål, toalettvann, preparater for badekar, antiseptiske midler, teaterspray, såper, noe som gjør syntetisk kamfer, smaksstoff.

Preparation

By treatment of camphene with acetic acid, usually in the presence of a catalyst; also by acetylation of isoborneol; depend[1]ing on the starting material (d-camphene or l-camphene), the resulting acetate may exhibit slight optical activity; the commercial product is considered to be optically inactive

Aroma terskelverdier

Aroma characteristics at 1.0%: camphoraceous woody,sweet, citrus and herbal with “Irish Spring” soapy nuances

Smakterskelverdier

Taste characteristics at 2 to 10 ppm: camphoraceous, woody, terpy and piney with a spicy, herbal and slightly citrus nuance


Isobornyl acetate Preparation Products And Raw materials


Raw materials

Eddiksyre is- -> Terpentinolje -> Metatitansyre -> (2S) -1- (3-Acetylthio-2-methyl-1-oxopropyl) -L-proline -> ALPHA-PINENE -> DL- Isoborneol


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